Carbon nanocages confined multicomponent phosphide heterostructures for boosting oxygen evolution reaction in alkaline water and seawater

被引:27
|
作者
Xu, Hui [1 ]
Jin, Lei [1 ]
Wang, Kun [1 ]
Yang, Lida [1 ]
He, Guangyu [1 ]
Chen, Haiqun [1 ]
机构
[1] Changzhou Univ, Adv Catalysis & Green Mfg Collaborat Innovat Ctr, Key Lab Adv Catalyt Mat & Technol, Changzhou 213164, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
FeNiCoP; Heterostructures; Carbon nanocages; Oxygen evolution reaction; BIMETALLIC PHOSPHIDE; ELECTROCATALYSTS; EFFICIENT; NANOPARTICLES; CATALYSTS;
D O I
10.1016/j.ijhydene.2023.05.254
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Transition metal phosphides (TMPs) have appealed tremendous interests in electro-catalytic oxygen evolution reaction (OER) due to its high intrinsic activity. Nevertheless, the poor electrochemical stability in harsh condition has seriously impeded their widespread application. Herein, we develop a facile strategy for realizing the substantial improvement in OER activity and stability by simultaneously engineering multicomponent phosphide heterostructure and introducing functionalized carbon nanocages. Profiting from the synergy of triple-phased heterostructure and the highly open hollow architecture, the MOF-derived Fe2P/Ni2P/NiCoP heterostructure functionalized carbon nanocages (FeNi-CoP@CNC) presents a favorable catalytic performance towards OER in 1 M KOH and alka-line seawater solutions with the low overpotentials of 237 and 245 mV at 10 mA cm-2, respectively, and no significant degradation is observed over long-term stability testing of 40 h. Detailed mechanism studies demonstrate that the triple-phased phosphide interface can facilitate the electron transfer and provide more catalytic active sites, while the functionalized carbon nanocages also boost the mass transfer and protect the FeNiCoP nanoparticles from aggregation.(c) 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:38324 / 38334
页数:11
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